Canonical Allele Identifier: PA2580449314
Gene: CDH23 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071407.4:p.Gly1076Ser
CA377143963
NM_022124.6:c.3226G>A